Hemoglobin

international journal for hemoglobin research

Volume 24, 2000 - Issue 3

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Original Article

Very Mild Pathology in a Case of Hb S/β˚-Thalassemia in Combination with a Homozygosity for the α-Thalassemia 3.7 kb Deletion

J. L. Kerkhoffs Leyenburg Hospital, The Hague, 2545 CH, The Netherlands

C. L. Harteveld MGC-Department of Human and Clinical Genetics, Leiden University Medical Center, 2233, AL Leiden, The Netherlands

P. Wijermans Leyenburg Hospital, The Hague, 2545 CH, The Netherlands

P. van Delft MGC-Department of Human and Clinical Genetics, Leiden University Medical Center, 2233, AL Leiden, The Netherlands

H. L. Haak Leyenburg Hospital, The Hague, 2545 CH, The Netherlands

L. F. Bernini MGC-Department of Human and Clinical Genetics, Leiden University Medical Center, 2233, AL Leiden, The Netherlands

P. C. Giordano MGC-Department of Human and Clinical Genetics, Leiden University Medical Center, 2233, AL Leiden, The NetherlandsCorrespondence[email protected]

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Citations (5)

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Maryam Neishabury, Christian Oberkanins, Lia Abbasi Moheb, Ali Akbar Pourfathollah, Kimia Kahrizi, Elahe Keyhany, Walter Krugluger & Hossein Najmabadi. (2003) High Prevalence of the −α3.7 Deletion Among Thalassemia Patients in Iran. Hemoglobin 27:1, pages 53-55.
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Articles from other publishers (4)

P. C. Giordano, W. Huisman & C. L. Harteveld. (2011) Iron Depletion: An Ameliorating Factor for Sickle Cell Disease?. ISRN Hematology 2011, pages 1-4.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 564 586 .

Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 435 436 .

Karen E Papez & William E Smoyer. (2004) Recent advances in congenital nephrotic syndrome. Current Opinion in Pediatrics 16:2, pages 165-170.
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Very Mild Pathology in a Case of Hb S/β˚-Thalassemia in Combination with a Homozygosity for the α-Thalassemia 3.7 kb Deletion

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Very Mild Pathology in a Case of Hb S/β˚-Thalassemia in Combination with a Homozygosity for the α-Thalassemia 3.7 kb Deletion

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Articles from other publishers (4)

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